Sunmark Iodides Tincture
Sunmark Iodides Tincture is an FDA drug label for the active ingredient ETHYL ALCOHOL manufactured by Strategic Sourcing Services LLC administered by TOPICAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20231219.
Generic: ETHYL ALCOHOL
Manufacturer: Strategic Sourcing Services LLC
Product Type: HUMAN OTC DRUG
Route: TOPICAL
Dosage Form:
NDC: 49348-711
Application: M003
Effective: 20231219
Active Ingredients: Active ingredient Ethyl Alcohol 48%
Indications & Usage
Use first aid to help prevent infection in minor cuts, scrapes and burns.
Dosage & Administration
Directions Clean the affected area. apply a small amount on the area 1 to 3 times daily. may be covered with sterile bandage. if bandaged, let dry first.
Contraindications
Not available.
Warnings
Warnings For external use only Flammable, keep away from fire or flame When using this product do not use in the eyes or apply over large areas of the body. In case of deep or puncture wounds, animal bites, or serious burns, consult a doctor. Stop use and consult doctor if the condition persists or gets worse. Do not use this product for longer than 1 week unless directed by a doctor. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Adverse Reactions
Not available.
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